Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 235,561,974 papers from all fields of science
Search
Sign In
Create Free Account
Polymicrogyria
Known as:
Polymicrogyria [Disease/Finding]
, Cerebral Polymicrogyrias
, Polymicrogyria, Cerebral
Expand
Heterogeneous disorders of cortical malformation characterized by excessive and small fused gyri and shallow sulci of the CORTEX with abnormal…
Expand
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
34 relations
Adams Oliver syndrome
BAND HETEROTOPIA
CK SYNDROME
CNS disorder
Expand
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Unusual early positive outcome of VNS therapy: anecdotal honeymoon or atypical prolonged immediate changes?
Marta De Rinaldis
,
N. Gigante
,
A. Trabacca
Acta Neurologica Belgica
2017
Corpus ID: 27843450
Vagus nerve stimulation (VNS) is indicated as an adjuvant to antiepileptic drugs in patients with drug-resistant epilepsy not…
Expand
2016
2016
Hemimegalencephaly with polymicrogyria – a case report
I. Raus
,
Mihaela Vintan
,
R. Coroiu
Clujul Medical
2016
Corpus ID: 18122561
Hemimegalencephaly on magnetic resonance imaging scan (MRI) consists of cortical gray matter almost uniformly abnormal, areas of…
Expand
2015
2015
MEGALENCEPHALY, POLYMICROGYRIA, POLYDACTYLY AND HYDROCEPHALUS (MPPH) SYNDROME: A NEW CASE WITH OCCIPITAL ENCEPHALOCELE AND CLEFT PALATE.
N. Demir
,
E. Peker
,
Gülşen I
,
S. Kaba
,
O. Tuncer
Genetic Counseling
2015
Corpus ID: 37243659
The megalencephaly, polymicrogyria, polydactyly, and hydrocephalus (MPPH) syndrome is quite rarely seen. The four main findings…
Expand
2008
2008
Micropolygyria: a histopathological and biochemical study.
C. Haberland
,
E. Brunngraber
Journal of mental deficiency research
2008
Corpus ID: 30402212
Review
2004
Review
2004
A Novel Signaling Mechanism in Brain Development
X. Piao
,
C. Walsh
Pediatric Research
2004
Corpus ID: 11366831
A review of: Piao X, Hill RS, Bodell A, Chang B., Basel-Vanagaite L., Straussberg R., Dobyns W. B., Qasrawi B., Winter R., Innes…
Expand
1990
1990
Autosomal recessive inheritance of polymicrogyria and dermatomyositis with paracrystalline inclusions.
J. D. Bleecker
,
J. D. Reuck
,
J. Martin
,
C. Ceuterick
,
D. Carton
,
J. Leroy
Clinical Neuropathology
1990
Corpus ID: 38803505
A 7-year-old mentally retarded girl died following subacute dermatomyositis. Muscle biopsies supported the clinical diagnosis and…
Expand
1985
1985
[An autopsy case of Prader-Labhart-Willi syndrome].
S. Hattori
,
S. Mochio
,
A. Kageyama
,
T. Nakajima
,
M. Akima
,
N. Fukunaga
No to shinkei = Brain and nerve
1985
Corpus ID: 23619504
An autopsy case of 23-years-old man with Prader-Labhart-Willi syndrome (P-L-W syndrome), who had died by acute renal failure due…
Expand
1984
1984
[2 autopsy cases of congenital muscular dystrophy of Fukuyama type--a typical and an atypical cases].
M. Koga
,
M. Abe
,
J. Tateishi
,
Y. Antoku
,
H. Iwashita
,
S. Miyoshino
No to shinkei = Brain and nerve
1984
Corpus ID: 13149110
Two autopsy cases of congenital muscular dystrophy of Fukuyama type (F-CMD) were described. The first case was diagnosed…
Expand
Review
1976
Review
1976
Confirmation of trisomy 22 by trypsin-giemsa staining.
M. Begleiter
,
P. Kulkarni
,
D. Harris
Journal of Medical Genetics
1976
Corpus ID: 10457109
A small-for-dates male infant with mental retardation, microcephaly, malformed ears, preauricular sinuses, epicanthal folds…
Expand
1970
1970
Syndrome of absent abdominal muscles: two cases with microcephaly, polymicrogyria, and cerebellar malformations
R. Heffner
Journal of Neurology Neurosurgery & Psychiatry
1970
Corpus ID: 16324126
Two unique cases of the syndrome of absent abdominal muscles with central nervous system involvement are presented. Microcephaly…
Expand